CSV Engineer

CSV Engineer    Reference:  TPS085
SALARY Negotiable   LOCATION County Cork, Carringtohill
JOB TYPE Contract (12 months)   DATE POSTED 08/04/2019
INDUSTRY Medical Device and Equipment manufacturer      
DESCRIPTION        
Client; Medical Devise and Equipment manufacturing company.

Responsibilities

Development of Validation Plans, Installation Qualifications (IQs), Operational Qualifications (OQs) and Summary Reports.

  • Prepare, execute, document and report validation protocols in line with GMP’s and other regulatory requirements and standards.
  • Assure that all validation test procedures are in line with current technology, corporate and governmental regulations.
  • Ensure that the Validation Strategy meets the quality requirements of its customers and applicable regulations FDA, EU & International Standards
  • Review and Approve validation protocols and assessments from a quality system documentation perspective.
  • Liaise with Engineering / Automation and external vendors regarding equipment documentation, HDS, SDS, FDS, User Requirement Specifications (URS’s), and any other associated validation issues.
  • Participate and communicate as required in project activities.
  • Develop procedures to manage computerised systems where required
  • Develop and present project plans to project management senior staff

Requirement

  • Bachelor of Science/Engineering degree or equivalent.
  • Knowledge of cGMP’s and other worldwide regulatory requirements.
  • Problem solving ability and excellent oral and written communications skills
  • Understanding of the computer system validation lifecycle

Preferred Qualifications

  • Candidates must have demonstrated experience in the delivery and management of IS / Automation systems in addition to a working knowledge of GAMP software development lifecycle, ANSI/ISA-S88 industry standards.
  • The successful candidate will have a least 3 years experience validating IS Automation systems for manufacturing organisations in the biotechnology or pharmaceutical industries.

 

Get in touch with us for full brief on this position.

 

Charlie Burgess +2081236574 Recruiter Agent in Automation UK & Ireland

Senior Automation Engineer

Senior Automation Engineer   Reference: TPS083
SALARY €70,000+   LOCATION Dublin, Ireland
JOB TYPE Permanent   DATE POSTED 18/03/2019
INDUSTRY Pharmaceutical

Medical Devise

     
         
DESCRIPTION        
Client: Pharmaceutical corporation operating a BioPharma facility in Dublin.

 

Requirement

Senior Automation Engineer , internally known as a Specialist IS (Information Systems) Automation Engineer, to join the Automation Engineering team reporting directly to the Senior Manager of Information Systems.

As a senior member of the Automation Engineering team, the Specialist will support complex and challenging process automation initiatives that require understanding of analytical problem-solving techniques, project management, life-cycle management and Operational Excellence. Additionally, the Specialist is responsible for providing project leadership and daily operational support to the Automation Engineering team at the site.

 

Responsibilities

  • Leads and supports of capital projects
  • Facilitates the application of advanced automation engineering principles in the design, specification, construction, startup, and validation of process and GMP utilities equipment and systems for capital projects of significant scope and complexity.
  • Leads and supports technical root cause analysis, incident investigations, and troubleshooting on process control issues related to electrical, instrumentation and control systems
  • Leads and supports new product introductions or new technology introductions by performing engineering assessments, implementing automation system configuration changes and supporting engineering runs
  • Devises new approaches to complex problems through adaptations and modifications of standard automation technical principles
  • Works closely with multiple disciplines, including manufacturing, process engineering, utility operations, maintenance, quality assurance, and validation to manage a diverse portfolio of projects.
  • Provides technical support to commercial and clinical manufacturing as needed.
  • Develops and executes strategic initiatives for long-range planning and lifecycle upgrades of various Automation platforms with activities including managing a 5 year roadmap of systems, presenting high level scope and cost estimates to executives for annual capital funding plan, and project management of initiatives once approved for execution
  • Provides mentorship to Automation Engineering team in daily operations
  • Communicates proactively with multiple levels within the organization, highlighting issues and proposing solutions

 

Qualifications

  • Bachelors Degree or Masters Degree in Chemical or Electrical Engineering or related technical field
  • 5+ years experience in Process Automation Engineering in a manufacturing support environment with at least 3+ years experience in the Pharmaceutical or Biotechnology industries
  • 5+ years combined experience with the following product platforms: Rockwell systems and/or Emerson DeltaV DCS systems
  • 5+ years experience with building automation systems with preference to Siemens Apogee or Desigo platforms
  • Programming expertise with SCADA, PLC, HMI, and wed based applications
  • Familiarity with industry standards for batch control systems, software development life cycle methodologies, S88, 21 CFR Part 11, Validation, and GAMP
  • Strong control system automation background. Design, installation, programming and validation of automated processes
  • Experience with Mammalian Cell Culture, Protein Purification, Clean Utilities, CIP, SIP, Production Services and non-GMP Utilities preferred

 

Get in touch with us for full brief on this position.

 

Charlie Burgess Recruiter 02081236574 Agent UK & Ireland

CSV Engineer

CVS Engineer   Reference:  TPS081
SALARY Negotiable LOCATION Dublin, Ireland
JOB TYPE Contract DATE POSTED 04/03/2019
INDUSTRY BioPharma
 
DESCRIPTION
Client; Engineering company focused on Process Automation delivery of Process Automation Solutions to Global Brands. Distilleries | Breweries | Blending Plants | Food Production | BioPharma.

End client; BioPharma corporation.

Responsibilities

Development of Validation Plans, Installation Qualifications (IQs), Operational Qualifications (OQs) and Summary Reports.

  • Prepare, execute, document and report validation protocols in line with GMP’s and other regulatory requirements and standards.
  • Assure that all validation test procedures are in line with current technology, corporate and governmental regulations.
  • Ensure that the Validation Strategy meets the quality requirements of its customers and applicable regulations FDA, EU & International Standards
  • Review and Approve validation protocols and assessments from a quality system documentation perspective.
  • Liaise with Engineering / Automation and external vendors regarding equipment documentation, HDS, SDS, FDS, User Requirement Specifications (URS’s), and any other associated validation issues.
  • Participate and communicate as required in project activities.
  • Develop procedures to manage computerised systems where required
  • Develop and present project plans to project management senior staff

Requirement

  • Bachelor of Science/Engineering degree or equivalent.
  • Knowledge of cGMP’s and other worldwide regulatory requirements.
  • Problem solving ability and excellent oral and written communications skills
  • Understanding of the computer system validation lifecycle

Preferred Qualifications

  • Candidates must have demonstrated experience in the delivery and management of IS / Automation systems in addition to a working knowledge of GAMP software development lifecycle, ANSI/ISA-S88 industry standards.
  • The successful candidate will have a least 3 years experience validating IS Automation systems for manufacturing organisations in the biotechnology or pharmaceutical industries.

 

Get in touch with us for full brief on this position.

 

Charlie Burgess Recruiter 02081236574 Agent UK